Isopropanol → 2,3-Dicyano-5-chloro-6-isopropoxypyrazine
Reaktionsgleichung
[C:1]([C:3]1[C:8]([C:9]#[N:10])=[N:7][C:6](Cl)=[C:5]([Cl:12])[N:4]=1)#[N:2].[CH:13]([OH:16])([CH3:15])[CH3:14]>>[C:9]([C:8]1[C:3]([C:1]#[N:2])=[N:4][C:5]([Cl:12])=[C:6]([O:16][CH:13]([CH3:15])[CH3:14])[N:7]=1)#[N:10]Komponenten
3
Versuchsvorschrift
Isopropanol (50 ml) was added to 1.99 g (0.01 mole) of 2,3-dicyano-5,6-dichloropyrazine, and the mixture was refluxed for 10 hours. After the reaction, the isopropanol was distilled off under reduced pressure. The crude product obtained (1.14 g) was chromatographed on a column of silica gel using benzene-n-hexane as an eluent to afford 1.00 g (yield 45%) of 2,3-dicyano-5-chloro-6-isopropoxypyrazine.
Aufarbeitung
- temperaturethe mixture was refluxed for 10 hours
- customAfter the reaction
- distillationthe isopropanol was distilled off under reduced pressure
- customThe crude product obtained (1.14 g)
- customwas chromatographed on a column of silica gel
Quellen und Nachweise
- ORD-Eintrag
- ord-4df73b6bddc7400ca2d7c4a93843c1b6
- Quelldatensatz
- uspto-grants-1984_07
- Patentnummer
- US04460403
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